Cardiovascular Effects of Sevelamer in Stage 3 CKD

Sevelamer
DOI: 10.1681/asn.2012070719 Publication Date: 2013-04-19T05:15:07Z
ABSTRACT
Serum phosphate independently predicts cardiovascular mortality in the general population and CKD, even when levels are normal range. Associations between serum phosphate, arterial stiffness, left ventricular (LV) mass suggest a possible pathophysiological mechanism, potentially mediated by phosphaturic hormone fibroblast growth factor-23 (FGF-23). To what extent binder sevelamer modulates these effects is not well understood. In this single-center, randomized, double-blind, placebo-controlled trial, we enrolled 120 patients with stage 3 nondiabetic CKD. After 4-week open-label run-in period, during which time all received carbonate, randomly assigned 109 to (n=55) or placebo (n=54) for an additional 36 weeks. We assessed LV systolic diastolic function magnetic resonance imaging echocardiography, stiffness carotid-femoral pulse wave velocity. The mean age was 55 years, eGFR 50 ml/min per 1.73 m(2). 40 weeks, found no statistically significant differences regard mass, function, Only 56% of subjects took ≥ 80% prescribed therapy; compliant subgroup, treatment associated lower urinary excretion FGF-23 but klotho, vitamin D, cardiovascular-related outcomes interest. conclusion, study does provide evidence that carbonate improves
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